Requirements for improving health and well‐being of children with Prader‐Willi syndrome and their families

Prader‐Willi syndrome (PWS) is a rare genetic condition with multi‐system involvement. The literature was reviewed to describe neurodevelopment and the behavioural phenotype, endocrine and metabolic disorders and respiratory and sleep functioning. Implications for child and family quality of life we...

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Detalles Bibliográficos
Autores principales: Mackay, Jessica, McCallum, Zoe, Ambler, Geoffrey R, Vora, Komal, Nixon, Gillian, Bergman, Philip, Shields, Nora, Milner, Kate, Kapur, Nitin, Crock, Patricia, Caudri, Daan, Curran, Jaqueline, Verge, Charles, Seton, Chris, Tai, Andrew, Tham, Elaine, Musthaffa, Yassmin, Lafferty, Antony R, Blecher, Greg, Harper, Jessica, Schofield, Cara, Nielsen, Aleisha, Wilson, Andrew, Leonard, Helen, Choong, Catherine S, Downs, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2019
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852695/
https://www.ncbi.nlm.nih.gov/pubmed/31257692
http://dx.doi.org/10.1111/jpc.14546

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852695/
https://www.ncbi.nlm.nih.gov/pubmed/31257692
http://dx.doi.org/10.1111/jpc.14546

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